BRPI0811639A2 - FENY CYCLOAKILAMINES REPLACED AS MONOAMINE RECAPTATION INHIBITORS - Google Patents

FENY CYCLOAKILAMINES REPLACED AS MONOAMINE RECAPTATION INHIBITORS

Info

Publication number
BRPI0811639A2
BRPI0811639A2 BRPI0811639-3A2A BRPI0811639A BRPI0811639A2 BR PI0811639 A2 BRPI0811639 A2 BR PI0811639A2 BR PI0811639 A BRPI0811639 A BR PI0811639A BR PI0811639 A2 BRPI0811639 A2 BR PI0811639A2
Authority
BR
Brazil
Prior art keywords
cycloakilamines
recaptation
feny
monoamine
inhibitors
Prior art date
Application number
BRPI0811639-3A2A
Other languages
Portuguese (pt)
Inventor
Liming Shao
Larry Wendel Hardy
Patrick Koch
Rudy Schreiber
Kerry L Spear
Fengjian Wang
Scott Christopher Malcolm
Michael Charles Hewitt
Jianguo Ma
Seth Ribe
Mark A Varney
Una Campbell
Sharon Rae Engel
Original Assignee
Sepracor Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sepracor Inc filed Critical Sepracor Inc
Publication of BRPI0811639A2 publication Critical patent/BRPI0811639A2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/42Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/52Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups or amino groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/76Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings and etherified hydroxy groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
BRPI0811639-3A2A 2007-05-31 2008-06-02 FENY CYCLOAKILAMINES REPLACED AS MONOAMINE RECAPTATION INHIBITORS BRPI0811639A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US94124207P 2007-05-31 2007-05-31
PCT/US2008/065571 WO2008151156A1 (en) 2007-05-31 2008-06-02 Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors

Publications (1)

Publication Number Publication Date
BRPI0811639A2 true BRPI0811639A2 (en) 2014-09-30

Family

ID=40094167

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0811639-3A2A BRPI0811639A2 (en) 2007-05-31 2008-06-02 FENY CYCLOAKILAMINES REPLACED AS MONOAMINE RECAPTATION INHIBITORS

Country Status (15)

Country Link
US (3) US8669291B2 (en)
EP (3) EP2154962A4 (en)
JP (3) JP5420534B2 (en)
KR (1) KR101581289B1 (en)
CN (3) CN101686672A (en)
AU (1) AU2008259841B2 (en)
BR (1) BRPI0811639A2 (en)
CA (1) CA2688493C (en)
HK (1) HK1200438A1 (en)
IL (1) IL202405A (en)
MX (1) MX2009012685A (en)
NZ (1) NZ580429A (en)
RU (1) RU2470011C2 (en)
WO (1) WO2008151156A1 (en)
ZA (1) ZA200907171B (en)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL380887A1 (en) * 2003-12-29 2007-04-02 Sepracor Inc. Pyrrole and pyrazole DAAO inhibitors
CA2614282A1 (en) 2005-07-06 2007-01-11 Sepracor Inc. Combinations of eszopiclone and trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-n-methyl-1-napthalenamine or trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine, and methods of treatment of menopause and mood, anxiety, and cognitive disorders
JP5438975B2 (en) 2006-01-06 2014-03-12 サノビオン ファーマシューティカルズ インク Tetralone monoamine reuptake inhibitor
ES2594156T3 (en) 2006-01-06 2016-12-16 Sunovion Pharmaceuticals Inc. Cycloalkylamines as monoamine reuptake inhibitors
WO2007115185A2 (en) 2006-03-31 2007-10-11 Sepracor Inc. Preparation of chiral amides and amines
US9108948B2 (en) 2006-06-23 2015-08-18 Abbvie Inc. Cyclopropyl amine derivatives
KR20090024811A (en) 2006-06-23 2009-03-09 아보트 러보러터리즈 Cyclopropyl amine derivatives as histamin h3 receptor modulators
US7884124B2 (en) * 2006-06-30 2011-02-08 Sepracor Inc. Fluoro-substituted inhibitors of D-amino acid oxidase
US7579370B2 (en) * 2006-06-30 2009-08-25 Sepracor Inc. Fused heterocycles
US20080082066A1 (en) * 2006-10-02 2008-04-03 Weyerhaeuser Co. Crosslinked carboxyalkyl cellulose fibers having non-permanent and temporary crosslinks
US7902252B2 (en) * 2007-01-18 2011-03-08 Sepracor, Inc. Inhibitors of D-amino acid oxidase
NZ580429A (en) 2007-05-31 2012-04-27 Sepracor Inc Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors
WO2010017418A1 (en) * 2008-08-07 2010-02-11 Sepracor Inc. Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase
US9186353B2 (en) 2009-04-27 2015-11-17 Abbvie Inc. Treatment of osteoarthritis pain
WO2011017634A2 (en) * 2009-08-07 2011-02-10 Sepracore Inc. Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase
WO2012037258A1 (en) 2010-09-16 2012-03-22 Abbott Laboratories Processes for preparing 1,2-substituted cyclopropyl derivatives
WO2014018563A2 (en) * 2012-07-23 2014-01-30 The Board Of Trustees Of The Leland Stanford Junior University Methods for the treatment of cancer
US9126891B2 (en) * 2014-01-29 2015-09-08 MediSynergics, LLC Cycloalkyl-diamines
US9381170B2 (en) * 2013-01-30 2016-07-05 MediSynergics, LLC Cycloalkyl-diamines for neurodegenerative disorders
US9283196B1 (en) * 2013-01-30 2016-03-15 MediSynergics, LLC Cycloalkyl-diamines for CNS disorders
JP2017523967A (en) * 2014-07-18 2017-08-24 バイエル・クロップサイエンス・アクチェンゲゼルシャフト Substituted vinyl cyanocycloalkanols, alkynyl cyanocycloalkanols, vinyl cyano heterocycloalkanols and alkynyl cyano heterocycloalkanols as activators against abiotic stresses in plants
MX2018012687A (en) * 2016-05-12 2019-01-31 Res Triangle Inst Vinylogous phenethylamines as neurotransmitter releasers.
JP2023528547A (en) 2020-05-29 2023-07-04 テグ-キョンプク メディカル イノベーション ファウンデーション A 5-membered heteroaryl derivative containing at least one N, and a pharmaceutical composition for use in preventing or treating a psychiatric disorder containing the same as an active ingredient
CN116057049A (en) 2020-05-29 2023-05-02 大邱庆北尖端医疗产业振兴财团 Carboxamide derivatives and pharmaceutical composition for preventing or treating mental diseases containing the same as active ingredient
US20230212121A1 (en) 2020-05-29 2023-07-06 Daegu-Gyeongbuk Medical Innovation Foundation Sulfonamide derivative and pharmaceutical composition comprising same as active ingredient for preventing or treating mental illness

Family Cites Families (160)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE616646A (en)
DE1124485B (en) 1960-02-12 1962-03-01 Hoechst Ag Process for the preparation of analeptically active phenylcycloalkylmethylamines
US3496181A (en) * 1966-10-24 1970-02-17 Upjohn Co 2 - aminocycloalkyl hydroquinones,esters,ethers and n-oxides thereof,and a process for preparing the same
GB1207731A (en) * 1968-05-14 1970-10-07 Reckitt & Sons Ltd Derivatives of pyrrolidine
US3536809A (en) 1969-02-17 1970-10-27 Alza Corp Medication method
US3598123A (en) 1969-04-01 1971-08-10 Alza Corp Bandage for administering drugs
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US3916899A (en) 1973-04-25 1975-11-04 Alza Corp Osmotic dispensing device with maximum and minimum sizes for the passageway
US3974157A (en) 1974-03-04 1976-08-10 Pennwalt Corporation 1-(Amino-alkyl)-2-aryl-cyclohexane alcohols and esters
US4008719A (en) 1976-02-02 1977-02-22 Alza Corporation Osmotic system having laminar arrangement for programming delivery of active agent
US4287212A (en) * 1976-04-30 1981-09-01 American Hoechst Corporation 2-Aryl-1,2-dialkylcycloalkylamines
JPS6033106B2 (en) 1977-10-07 1985-08-01 住友化学工業株式会社 Carboxylic acid esters, their production methods, and insecticides and acaricides containing them as active ingredients
ZA817261B (en) 1980-10-23 1982-09-29 Schering Corp Carboxyalkyl dipeptides,processes for their production and pharmaceutical compositions containing them
ZA829562B (en) * 1982-02-09 1983-10-26 Upjohn Co 2-(phenylmethylene)cycloalkylamines and-azetidines
US4540690A (en) * 1982-02-09 1985-09-10 The Upjohn Company 2-(Phenylmethylene)cycloalkylamines and -azetidines
JPS58177915A (en) 1982-04-12 1983-10-18 Green Cross Corp:The Antithrombotic agent
EP0152032B1 (en) 1984-02-03 1988-10-26 Olympus Optical Co., Ltd. Calculus crushing apparatus
JPS60172970A (en) * 1984-02-15 1985-09-06 Shionogi & Co Ltd Cis-azolylcycloalkanol derivative, its preparation and fungicide for agricultural use
EP0190224A1 (en) 1984-07-30 1986-08-13 Schering Corporation PROCESS FOR THE PREPARATION OF CIS, ENDOOCTAHYDROCYCLOPENTA [b] PYRROLE-2-CARBOXYLATE
DE3431541A1 (en) 1984-08-28 1986-03-06 Hoechst Ag, 6230 Frankfurt CIS, ENDO-2-AZABICYCLOALKAN-3-CARBONIC ACID DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, THEIR USE AND INTERMEDIATE PRODUCTS IN THEIR PRODUCTION
IE58110B1 (en) 1984-10-30 1993-07-14 Elan Corp Plc Controlled release powder and process for its preparation
US4738709A (en) 1985-01-10 1988-04-19 Ppg Industries, Inc. Herbicidally active substituted benzisoxazoles
US4751231A (en) 1987-09-16 1988-06-14 Merck & Co., Inc. Substituted thieno[2,3-b]pyrrole-5-sulfonamides as antiglaucoma agents
JPH01172388A (en) 1987-12-25 1989-07-07 Sumitomo Chem Co Ltd Thieno(3,2-b)pyrrolo(2,3-d)pyrroles and production thereof
US5073543A (en) 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
US4981870A (en) 1989-03-07 1991-01-01 Pfizer Inc. Use of 4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine derivatives in the treatment of psychosis, inflammation and as immunosuppressants
IT1229203B (en) 1989-03-22 1991-07-25 Bioresearch Spa USE OF 5 METHYLTHETRAHYDROPHOLIC ACID, 5 FORMYLTHETRAHYDROPHOLIC ACID AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITIONS IN THE FORM OF CONTROLLED RELEASE ACTIVE IN THE THERAPY OF MENTAL AND ORGANIC DISORDERS.
PT93943A (en) 1989-05-05 1991-02-08 Searle & Co PROCESS FOR THE PREPARATION OF COMPOUNDS CONTAINING INDOLE-2-CARBOXYLATE COMPOUNDS FOR TREATMENT OF CNS DISTURBACTIONS
ATE172712T1 (en) 1989-05-31 1998-11-15 Upjohn Co CNS-ACTIVE 8-HETEROCYCLYL-2-AMINOTETRALIN DERIVATIVES
US5120548A (en) 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
ATE126511T1 (en) 1990-02-02 1995-09-15 Schering Corp 4,5-CYCLOALKANO-3-BENZAZEPINE-7-OL DERIVATIVES AND THEIR USE.
US5733566A (en) 1990-05-15 1998-03-31 Alkermes Controlled Therapeutics Inc. Ii Controlled release of antiparasitic agents in animals
JPH0477476A (en) 1990-07-19 1992-03-11 Sankyo Co Ltd Antiulcer agent
US5086054A (en) 1990-07-31 1992-02-04 Sri International Novel arylcycloalkanepolyalkylamines
JP3007138B2 (en) 1990-11-27 2000-02-07 ファイザー製薬株式会社 Novel hydroxamic acid and N-hydroxyurea derivatives and compositions thereof
US5580578A (en) 1992-01-27 1996-12-03 Euro-Celtique, S.A. Controlled release formulations coated with aqueous dispersions of acrylic polymers
GB9208492D0 (en) 1992-04-16 1992-06-03 Glaxo Spa Heterocyclic compounds
EP0665226A1 (en) 1992-10-28 1995-08-02 Toyama Chemical Co., Ltd. Novel 1,2-benzisoxazole derivative or salt thereof, and brain protective agent comprising the same
US5591767A (en) 1993-01-25 1997-01-07 Pharmetrix Corporation Liquid reservoir transdermal patch for the administration of ketorolac
GB9304500D0 (en) 1993-03-05 1993-04-21 Glaxo Spa Heterocyclic compounds
ES2081747B1 (en) 1993-09-07 1997-01-16 Esteve Labor Dr AMIDES DERIVED FROM TIENOPIRROLES, THEIR PREPARATION AND THEIR APPLICATION AS MEDICINES.
GB9321221D0 (en) 1993-10-14 1993-12-01 Glaxo Spa Heterocyclic compounds
GB9326284D0 (en) 1993-12-23 1994-02-23 Erba Carlo Spa Pyrrolydenemethyl-derivatives and process for their preparation
IT1270594B (en) 1994-07-07 1997-05-07 Recordati Chem Pharm CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION OF LIQUID SUSPENSION MOGUISTEIN
CN1047384C (en) 1994-07-28 1999-12-15 北京大学 Synthetic process of Ramipril
MX9701630A (en) 1994-08-30 1997-06-28 Sankyo Co Isoxazoles.
US5484763A (en) 1995-02-10 1996-01-16 American Cyanamid Company Substituted benzisoxazole and benzisothiazole herbicidal agents
US5620997A (en) 1995-05-31 1997-04-15 Warner-Lambert Company Isothiazolones
US5859042A (en) 1995-09-27 1999-01-12 Ono Pharmaceutical Co., Ltd. Five membered heterocyclic compounds
CZ126598A3 (en) 1995-10-26 1998-09-16 Mitsubishi-Tokyo Pharmaceuticals, Inc. Phenylethanolamine compounds, process of their preparation and pharmaceutical compositions containing thereof
CZ289340B6 (en) * 1996-01-31 2002-01-16 Byk Gulden Lomberg Chemische Fabrik Gmbh Phenanthridine derivatives and pharmaceutical preparations in which they are comprised
DE19711785A1 (en) 1997-03-21 1998-09-24 Merck Patent Gmbh Endothelin receptor antagonists
US6503582B1 (en) 1997-08-19 2003-01-07 Mattel, Inc. Fluid-swellable composition, device and method for using the same
GB9717804D0 (en) 1997-08-22 1997-10-29 Zeneca Ltd Chemical compounds
WO1999018065A1 (en) 1997-10-03 1999-04-15 Chirotech Technology Limited Chiral amines
GB9803226D0 (en) 1998-02-17 1998-04-08 Zeneca Ltd Chemical compounds
GB9803228D0 (en) 1998-02-17 1998-04-08 Zeneca Ltd Chemical compounds
JP2002507598A (en) 1998-03-26 2002-03-12 スージェン・インコーポレーテッド A family of heterocyclic compounds for regulating tyrosine protein kinase
US6476078B2 (en) 1999-08-11 2002-11-05 Sepracor, Inc. Methods of using sibutramine metabolites in combination with a phosphodiesterase inhibitor to treat sexual dysfunction
US6632836B1 (en) 1998-10-30 2003-10-14 Merck & Co., Inc. Carbocyclic potassium channel inhibitors
CN1329590A (en) * 1998-12-02 2002-01-02 达尔文发现有限公司 Therapeutic product and its use
US6828460B2 (en) * 1999-03-22 2004-12-07 Pfizer Inc. Resorcinol derivatives
DE19915601A1 (en) * 1999-04-07 2000-10-19 Gruenenthal Gmbh 3-Amino-3-arylpropan-1-ol derivatives, their preparation and use
FR2795733B1 (en) 1999-06-30 2001-09-07 Aventis Pharma Sa STREPTOGRAMIN DERIVATIVES, THEIR PREPARATION AND THE COMPOSITIONS CONTAINING THEM
EP1391460A1 (en) 1999-09-30 2004-02-25 Pfizer Products Inc. Tricyclic pyrrolyl amides as glycogen phosphorylase inhibitors
DE60007592T2 (en) 1999-09-30 2004-09-16 Pfizer Products Inc., Groton Bicyclic pyrrolylamides as glycogen phosphorylase inhibitors
IL148820A0 (en) 1999-10-08 2002-09-12 Smithkline Beecham Corp Fab i inhibitors
ATE402140T1 (en) * 1999-12-08 2008-08-15 Lilly Co Eli CYCLOPENTYL SULFONAMIDE DERIVATIVES
DE19960917A1 (en) 1999-12-17 2001-06-21 Bayer Ag New 3-oxo-2,1-benzisoxazol-1 (3H) -carboxamides for the treatment of CNS diseases
DE10000312A1 (en) 2000-01-05 2001-07-12 Gruenenthal Gmbh Substituted aminomethyl phenyl cyclohexane derivatives
US6632417B2 (en) 2000-03-07 2003-10-14 Chevron U.S.A. Inc. Process for preparing zeolites
JP2001247462A (en) 2000-03-07 2001-09-11 Otsuka Pharmaceut Co Ltd Urease inhibitor
EP1136071A3 (en) 2000-03-22 2003-03-26 Pfizer Products Inc. Use of glycogen phosphorylase inhibitors
WO2001079208A1 (en) 2000-04-19 2001-10-25 Kaneka Corporation Novel azetidine derivative and process for preparation thereof
GB0012214D0 (en) 2000-05-19 2000-07-12 Merck Sharp & Dohme Therapeutic agents
AU2001280461A1 (en) 2000-08-04 2002-02-18 Eli Lilly And Company Substituted pyrrole compounds and their use as spla2 inhibitors
GB0021831D0 (en) 2000-09-06 2000-10-18 Astrazeneca Ab Chemical compounds
DE10049481A1 (en) 2000-09-29 2002-05-02 Gruenenthal Gmbh Substituted C-cyclohexylmethylamine derivatives
DE10049483A1 (en) * 2000-09-29 2002-05-02 Gruenenthal Gmbh Substituted 1-aminobutan-3-ol derivatives
AU2000277557A1 (en) 2000-10-06 2002-04-22 Smith Kline Beecham Corporation Methods of agonizing and antagonizing fabk
WO2002032858A1 (en) * 2000-10-13 2002-04-25 Eli Lilly And Company Cycloalkylfluorosulfonamide derivatives
SE0003810D0 (en) 2000-10-20 2000-10-20 Pharmacia Ab Novel compounds their use and preparations
TWI283575B (en) 2000-10-31 2007-07-11 Eisai Co Ltd Medicinal compositions for concomitant use as anticancer agent
DE10063992A1 (en) 2000-12-21 2002-07-04 Max Planck Gesellschaft Tryptophan analogues in proteins, peptides and peptide lead structures
US6372919B1 (en) 2001-01-11 2002-04-16 Dov Pharmaceutical, Inc. (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane, compositions thereof, and uses as an anti-depressant agent
US20020123490A1 (en) 2001-03-01 2002-09-05 Pfizer Inc. Combination treatment for anxiety, depression, obsessive compulsive disorder and psychosis
US7365205B2 (en) 2001-06-20 2008-04-29 Daiichi Sankyo Company, Limited Diamine derivatives
GB0115602D0 (en) 2001-06-26 2001-08-15 Syngenta Participations Ag Organic compounds
DE10132747A1 (en) * 2001-07-05 2003-01-23 Gruenenthal Gmbh Substituted 1-aryl-but-3-enylamine and 1-aryl-but-2-enylamine compounds
US6603000B2 (en) 2001-07-11 2003-08-05 Boehringer Ingelheim Pharmaceuticals, Inc. Synthesis for heteroarylamine compounds
MXPA04001272A (en) 2001-08-09 2004-05-27 Daiichi Seiyaku Co Diamine derivatives.
US7045543B2 (en) 2001-11-05 2006-05-16 Enzrel Inc. Covalent conjugates of biologically-active compounds with amino acids and amino acid derivatives for targeting to physiologically-protected sites
WO2003039540A2 (en) 2001-11-09 2003-05-15 Sepracor Inc. D-amino acid oxidase inhibitors for learning and memory
US6780891B2 (en) * 2001-11-30 2004-08-24 Sepracor Inc. Tramadol analogs and uses thereof
DE10164581A1 (en) * 2001-12-14 2003-06-26 Gruenenthal Gmbh Medicaments that inhibit noradrenaline reuptake, useful e.g. for treating emesis, diarrhea, inflammation, depression or especially pain, comprise new or known cyclic aminomethyl-substituted alcohols
DE10161809A1 (en) * 2001-12-14 2003-06-26 Gruenenthal Gmbh Pharmaceutical compositions, useful e.g. for the treatment of neurodegenerative diseases, psychiatric or neuropathological diseases or especially pain and epilepsy, comprise N,N'-disubstituted piperazine derivatives
TW200307539A (en) 2002-02-01 2003-12-16 Bristol Myers Squibb Co Cycloalkyl inhibitors of potassium channel function
DE60327691D1 (en) * 2002-02-11 2009-07-02 Rhodia Chimie Sa DETERGENT WITH BLOCK COPOLYMER
GB0205170D0 (en) 2002-03-06 2002-04-17 Astrazeneca Ab Chemical compounds
GB0205165D0 (en) 2002-03-06 2002-04-17 Astrazeneca Ab Chemical compounds
US6995144B2 (en) 2002-03-14 2006-02-07 Eisai Co., Ltd. Nitrogen containing heterocyclic compounds and medicines containing the same
AU2003227360A1 (en) 2002-04-25 2003-11-10 Yamanouchi Pharmaceutical Co., Ltd. Novel amide derivatives or salts thereof
AU2003236247A1 (en) 2002-05-03 2003-11-17 Warner-Lambert Company Llc Bombesin antagonists
FR2841487B1 (en) 2002-06-26 2004-08-20 Solystic METHOD FOR DETECTING SINGLE PLIERS AND MULTIPLE PLUG PLUGS IN A POSTAL SORTING FACILITY
DE10233048A1 (en) 2002-07-19 2004-01-29 Grünenthal GmbH Use of 1-phenyl-3dimethylamino-propane compounds for the treatment of depressive symptoms
US20050182131A1 (en) * 2002-07-19 2005-08-18 Gruenenthal Gmbh 1-Phenyl-2-dimethylaminomethyl cyclohexane compounds and therapies for depressive symptoms, pain and incontinence
AU2003252299A1 (en) 2002-07-31 2004-02-16 Eisai Co., Ltd. Novel physiologically active substance
US7537891B2 (en) 2002-08-27 2009-05-26 Bristol-Myers Squibb Company Identification of polynucleotides for predicting activity of compounds that interact with and/or modulate protein tyrosine kinases and/or protein tyrosine kinase pathways in breast cells
DE60305052T2 (en) 2002-09-06 2006-12-21 Janssen Pharmaceutica N.V. THIENOPYRROLYL AND FURANOPYRROLYL COMPOUNDS AND THEIR USE AS HISTAMINE H4 RECEPTOR LIGANDS
MXPA05002700A (en) 2002-09-16 2005-09-08 Sepracor Inc Treatment of cns disorders with trans.
US20040087661A1 (en) 2002-09-16 2004-05-06 Sepracor, Inc. Treatment of CNS disorders with trans 4-3(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-napthalenamine
TW200418838A (en) * 2002-09-18 2004-10-01 Bristol Myers Squibb Co Compounds for the treatment of premature ejaculation
GB0222912D0 (en) 2002-10-03 2002-11-13 Astrazeneca Ab Novel process and intermediates
JP2006504795A (en) 2002-10-03 2006-02-09 サイプレス バイオサイエンス, インコーポレイテッド Step-by-step escalation of antidepressant dosage to treat neurological disorders and daily divided doses
GB0222909D0 (en) 2002-10-03 2002-11-13 Astrazeneca Ab Novel process and intermediates
US20040097554A1 (en) 2002-10-30 2004-05-20 Pfizer Inc Heteroaryl-hexanoic acid amide derivatives as immonomodulatory agents
WO2004041780A2 (en) 2002-11-07 2004-05-21 Pfizer Products Inc. N-(indole-2-carbonyl) amides as anti-diabetic agents
US7345180B2 (en) 2003-01-31 2008-03-18 Sanwa Kagaku Kenkyusho Co., Ltd. Compound inhibiting dipeptidyl peptidase IV
ATE482747T1 (en) 2003-04-11 2010-10-15 High Point Pharmaceuticals Llc NEW AMIDE DERIVATIVES AND THEIR PHARMACEUTICAL USES
CA2521962A1 (en) 2003-04-30 2004-11-11 Pfizer Products Inc. Anti-diabetic agents
WO2004113345A1 (en) 2003-06-20 2004-12-29 Japan Tobacco Inc. Fused pyrrole compound and medicinal use thereof
ATE360638T1 (en) 2003-06-30 2007-05-15 Servier Lab METHOD FOR THE SYNTHESIS OF PERINDOPRIL AND ITS PHARMACEUTICALLY SUITABLE SALTS
JP4745226B2 (en) 2003-07-07 2011-08-10 チバ ホールディング インコーポレーテッド Production of flopirole
SG145693A1 (en) 2003-07-29 2008-09-29 Signature R & D Holdings Llc Amino acid prodrugs
GB0318463D0 (en) 2003-08-07 2003-09-10 Astrazeneca Ab Chemical compounds
GB0319759D0 (en) 2003-08-22 2003-09-24 Astrazeneca Ab Chemical compounds
WO2005020986A1 (en) 2003-08-29 2005-03-10 Astrazeneca Ab Heterocyclic amide derivatives which posses glycogen phosphorylase inhibitory activity
GB0320422D0 (en) 2003-08-30 2003-10-01 Astrazeneca Ab Chemical compounds
KR100798161B1 (en) 2003-10-23 2008-01-28 에프. 호프만-라 로슈 아게 Triaza-spiropiperidine derivatives for use as glyt-1 inhibitors in the treatment of neurological and neuropsychiatric disorders
US7396940B2 (en) 2003-10-23 2008-07-08 Hoffmann-La Roche Inc. Combinatorial library of 3-aryl-1H-indole-2-carboxylic acid
SI1420028T1 (en) 2003-11-19 2007-06-30 Servier Lab Method for synthesis of perindopril and its pharmaceutically acceptable salts
BRPI0417910A (en) 2003-12-29 2007-04-10 Sepracor Inc compound or a pharmaceutically acceptable salt or salvate thereof, and use of a compound
PL380887A1 (en) 2003-12-29 2007-04-02 Sepracor Inc. Pyrrole and pyrazole DAAO inhibitors
US20070197610A1 (en) 2004-03-16 2007-08-23 Janssen Pharmaceutica N.V. Benzisoxazoles
GEP20094826B (en) 2004-05-07 2009-11-10 Warner Lambert Co 3- or 4-monosubstituted phenol and thiophenol derivatives useful as h3 ligands
MXPA06013270A (en) * 2004-05-14 2007-04-23 Johnson & Johnson Carboxamido opioid compounds.
CA2567851A1 (en) * 2004-05-21 2006-01-05 Merck & Co., Inc. Amino cyclopentyl heterocyclic and carbocyclic modulators of chemokine receptor activity
TWI335816B (en) 2004-05-26 2011-01-11 Eisai R&D Man Co Ltd Cinnamide compound
WO2005123677A1 (en) 2004-06-16 2005-12-29 Actelion Pharmaceuticals Ltd 4-carbonyl substituted 1,1,2-trimethyl-1a,4,5,5a-tetrahydro-1h-4-aza-cyclopropa'a!pentalene derivatives as agonists for the g-protein-coupled receptor s1p1/edg1 and immunosuppressive agents
CN102827082B (en) 2004-07-01 2015-01-07 第一三共株式会社 Thienopyrazole derivative having PDE7 inhibitory activity
US7276631B2 (en) * 2004-07-20 2007-10-02 Bristol-Myers Squibb Company Cyclopentylamine and cyclohexylamine derivatives as NK-1/SSRI antagonists
JO2629B1 (en) 2004-08-19 2012-06-24 افينتيس فارما سوتيكالز انك Substituted Thenopyrrole carboxylic acid amids, Pyrrolothiazole carboxylic acid amids,and related analogs as inhibitors of casein kinase I epsilon
US7411093B2 (en) * 2004-12-20 2008-08-12 Hoffman-La Roche Inc. Aminocycloalkanes as DPP-IV inhibitors
EP1844051A1 (en) 2005-01-19 2007-10-17 Biolipox AB Thienopyrroles useful in the treatment of inflammation
CN100391945C (en) 2005-05-31 2008-06-04 浙江大学 S-(-)-indolyl-2-carboxylic acid synthesizing method
CA2624795A1 (en) 2005-10-06 2007-04-12 Merck Sharp & Dohme Limited Use of fused pyrrole carboxylic acids for the treatment of neurodegenerative and psychiatric diseases as d-amino acid oxidase inhibitors
UA95788C2 (en) 2005-12-15 2011-09-12 Ф. Хоффманн-Ля Рош Аг Fused pyrrole derivatives
JP5438975B2 (en) 2006-01-06 2014-03-12 サノビオン ファーマシューティカルズ インク Tetralone monoamine reuptake inhibitor
ES2594156T3 (en) 2006-01-06 2016-12-16 Sunovion Pharmaceuticals Inc. Cycloalkylamines as monoamine reuptake inhibitors
WO2007115185A2 (en) 2006-03-31 2007-10-11 Sepracor Inc. Preparation of chiral amides and amines
US7884124B2 (en) 2006-06-30 2011-02-08 Sepracor Inc. Fluoro-substituted inhibitors of D-amino acid oxidase
WO2008005456A2 (en) 2006-06-30 2008-01-10 Sepracor Inc. Fused heterocyclic inhibitors of d-amino acid oxidase
US7579370B2 (en) 2006-06-30 2009-08-25 Sepracor Inc. Fused heterocycles
US20080058395A1 (en) 2006-06-30 2008-03-06 Sepracor Inc. Fused heterocyclic inhibitors of D-amino acid oxidase
CN1962656A (en) 2006-11-29 2007-05-16 沈阳药科大学 Indomethacin 5-fluorouracil methyl ester pharmaceutical compound and its formulation and preparation method
WO2008079382A1 (en) * 2006-12-21 2008-07-03 Abbott Laboratories Sphingosine-1 -phosphate receptor agonist and antagonist compounds
WO2008089453A2 (en) 2007-01-18 2008-07-24 Sepracor Inc. Inhibitors of d-amino acid oxidase
US7902252B2 (en) 2007-01-18 2011-03-08 Sepracor, Inc. Inhibitors of D-amino acid oxidase
NZ580429A (en) * 2007-05-31 2012-04-27 Sepracor Inc Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors
WO2010017418A1 (en) 2008-08-07 2010-02-11 Sepracor Inc. Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase

Also Published As

Publication number Publication date
EP3296289A3 (en) 2018-06-20
CN101686672A (en) 2010-03-31
EP2617704B1 (en) 2017-06-28
MX2009012685A (en) 2009-12-14
EP3296289A2 (en) 2018-03-21
US9586888B2 (en) 2017-03-07
JP2016065085A (en) 2016-04-28
US20140121282A1 (en) 2014-05-01
EP2154962A1 (en) 2010-02-24
ZA200907171B (en) 2010-12-29
AU2008259841B2 (en) 2015-02-05
KR20100019982A (en) 2010-02-19
JP2010529045A (en) 2010-08-26
RU2009149292A (en) 2011-07-10
RU2470011C2 (en) 2012-12-20
CA2688493A1 (en) 2008-12-11
JP2014062108A (en) 2014-04-10
AU2008259841A1 (en) 2008-12-11
WO2008151156A1 (en) 2008-12-11
JP5420534B2 (en) 2014-02-19
IL202405A0 (en) 2010-06-30
US20090005456A1 (en) 2009-01-01
IL202405A (en) 2014-05-28
KR101581289B1 (en) 2015-12-31
CN108178733A (en) 2018-06-19
US8669291B2 (en) 2014-03-11
NZ580429A (en) 2012-04-27
CN103936605B (en) 2017-09-01
US20170204050A1 (en) 2017-07-20
EP2154962A4 (en) 2012-08-15
HK1200438A1 (en) 2015-08-07
CN103936605A (en) 2014-07-23
CA2688493C (en) 2016-04-19
EP2617704A1 (en) 2013-07-24

Similar Documents

Publication Publication Date Title
BRPI0811639A2 (en) FENY CYCLOAKILAMINES REPLACED AS MONOAMINE RECAPTATION INHIBITORS
CY2020024I1 (en) BETA-LACTAMAS INHIBITORS
BRPI0811065A2 (en) 5-HETEROARYL INDAZOES REPLACED AS KINASE INHIBITORS
BRPI0913879A2 (en) phenylpyrazinones as kinase inhibitors
BRPI0812825A2 (en) FTAAZINONE DERIVATIVES AS PARP-1 INHIBITORS
BRPI0920135A2 (en) imidazopyridazinecarbonitriles useful as kinase inhibitors
BRPI0811044A2 (en) 2-MORFOLIN-4-IL-PYRIMIDINES AS P13K INHIBITORS.
DK2634231T3 (en) COMPOSITIONS
BRPI0921327A2 (en) Herbicide-Protector Combination
BRPI0906749A2 (en) Composition
BRPI0913808A2 (en) composition
DK2229572T3 (en) recuperator
BRPI0917231A2 (en) composition
DK2344471T3 (en) 7-piperidinealkyl-3,4-dihydroquinolone DERIVATIVE
BRPI0814797A2 (en) DNA-PK INHIBITORS
BRPI0920053A2 (en) pyrazolylaminopyridines as fak inhibitors
BRPI0918564A2 (en) inhibitors
BR112012001070A2 (en) complement activation inhibitors
BRPI1011901A2 (en) photoinitiators
BRPI0716198A2 (en) PYROROLO-ISOKINOLINES AS KINASE INHIBITORS
BRPI1005318A2 (en) composition
BRPI0922728A2 (en) herbicide-antidote combination
DK2379722T3 (en) expression
BRPI0909425A2 (en) hydroxyquinoxalinecarboxamide derivative
BRPI0914936A2 (en) naphthyridininones as aurora kinase inhibitors

Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]
B08G Application fees: restoration [chapter 8.7 patent gazette]
B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B06T Formal requirements before examination [chapter 6.20 patent gazette]
B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]

Free format text: DE ACORDO COM O ARTIGO 229-C DA LEI NO 10196/2001, QUE MODIFICOU A LEI NO 9279/96, A CONCESSAO DA PATENTE ESTA CONDICIONADA A ANUENCIA PREVIA DA ANVISA. CONSIDERANDO A APROVACAO DOS TERMOS DO PARECER NO 337/PGF/EA/2010, BEM COMO A PORTARIA INTERMINISTERIAL NO 1065 DE 24/05/2012, ENCAMINHA-SE O PRESENTE PEDIDO PARA AS PROVIDENCIAS CABIVEIS.

B15K Others concerning applications: alteration of classification

Free format text: A CLASSIFICACAO ANTERIOR ERA: A01N 43/00

Ipc: A61K 31/135 (2006.01), A61P 25/24 (2006.01), A61P

B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 13A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2622 DE 06/04/2021.